Synthesis of barium titanate nanocrystals decorated with PtO for enhanced photooxidative desulfurization of thiophene

被引:1
作者
Alshaikh, Hind [1 ]
Mohamed, Reda M. [2 ]
机构
[1] King Abdulaziz Univ, Coll Sci & Arts, Dept Chem, Rabigh 21911, Saudi Arabia
[2] King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80200, Jeddah 21589, Saudi Arabia
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2025年 / 314卷
关键词
PtO; BaTiO3; Photocatalysis; Thiophene; Oxidative desulfurization; VISIBLE-LIGHT-DRIVEN; PHOTOCATALYTIC ACTIVITY; OXIDATIVE DESULFURIZATION; MOLECULAR-OXYGEN; NANOTUBE ARRAYS; HETEROJUNCTION; BATIO3; TIO2; NANOPARTICLES; PERFORMANCE;
D O I
10.1016/j.mseb.2025.118028
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Perovskite titanates have emerged as promising photocatalysts for environmental remediation. One particular challenge is the removing of sulfur-containing compounds like thiophene (TPH) from fuels. Herein, we synthesized mesoporous BaTiO3 (BTO) nanostructures using a surfactant-assisted hydrothermal method and subsequently modified with varying amounts (0.5-2.0 wt%) of PtO nanoparticles (NPs) to form PtO-BTO composites. The characterization of the composite materials reveals a mesoporous structure that enhances their optical properties after adding PtO NPs. Specifically, incorporating 1.5 wt% PtO significantly reduced the bandgap energy (Eg) from 2.68 to 1.93 eV, leading to improved visible light absorption. This composite demonstrated superior photocatalytic performance, achieving complete photooxidative desulfurization of TPH during 90 min under visible light irradiation, with a remarkable oxidation rate constant of 0.035 min-1 . Moreover, the photocatalyst exhibited excellent recyclability. Photoluminescence and photocurrent measurements confirmed that the introduction of PtO effectively suppressed charge carrier recombination. The proposed photoconversion mechanism involves a step-scheme charge transfer process facilitated by the heterojunction between PtO and BTO. This mechanism enables effective charge isolation and transfer, resulting in increased photocatalytic activity. This research accentuates the potential of BaTiO3-based photocatalysts for use in fuel processing and corresponding industries.
引用
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页数:11
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